UDI device identifier
Alaris, SmartSite 2432-0007
UDI device identifier 10885403232329 · BD Switzerland Sàrl
Key facts
| Primary DI | 10885403232329 |
|---|---|
| Brand name | Alaris, SmartSite |
| Version or model | 2432-0007 |
| Catalog number | 2432-0007 |
| Company | BD Switzerland Sàrl |
| DUNS number | 482631558 |
| Product code | FPA |
| GMDN term | Electric infusion pump administration set, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 22, 2016 |
| Version date | Oct 6, 2026 |
| Description | Pump Infusion Set, 0.2 Micron Filter, Back Check Valve, 3 Y-Sites, 297 cm, (117 in) |
At a glance
- 100–999 MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: